Evidence map›Paper›PMID 32733068›Full record

ReviewOncogene2020

Targeting telomerase for cancer therapy.

Adam N Guterres, Jessie Villanueva

Open access · greenAbstract readReview
In one paragraph

Review in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed
15.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

135 citing papers in PubMed, 261 citations in OpenAlex.

  1. Review
  2. Potential of hTERT mRNA for the management of advanced head and neck squamous cell carcinoma.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026
    Article
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  6. Review
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  9. Review
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  11. Review
  12. Endometriosis and the Hallmarks of Cancer.Reproductive sciences (Thousand Oaks, Calif.) · 2026
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Role ofMolecular and clinical oncology · 2025
    Review

75 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Adam N GuterresMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-4607-2099
Jessie VillanuevaMolecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, PA, USA. jvillanueva@wistar.org.ORCID http://orcid.org/0000-0001-5701-2609
The Wistar Institute · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Targeting the MAP and PI3 Kinase Pathways in MelanomaP01CA114046 · NCI · WISTAR INSTITUTE · PI MURPHY, MAUREEN E. · 2008 to 2023
$37.1M
Targeted Combination Therapy for MelanomaP50CA174523 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$11.1M
Development of BRAF Dimer Inhibitors to Treat Drug Resistant MelanomaR01CA226888 · NCI · UNIVERSITY OF PENNSYLVANIA · PI MARMORSTEIN, RONEN, WINKLER, JEFFREY D · 2019 to 2023
$3.4M
Targeting TERT in MelanomaR01CA215733 · NCI · WISTAR INSTITUTE · PI VILLANUEVA, JESSIE · 2017 to 2021
$2.4M
NCI NIH HHS P01 CA114046NCI NIH HHS P30 CA010815NCI NIH HHS P50 CA174523NCI NIH HHS R01 CA215733NCI NIH HHS R01 CA226888U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P01CA114046U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P50CA174523U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA215733U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA226888
6 · The paper itself

Abstract

Telomere maintenance via telomerase reactivation is a nearly universal hallmark of cancer cells which enables replicative immortality. In contrast, telomerase activity is silenced in most adult somatic cells. Thus, telomerase represents an attractive target for highly selective cancer therapeutics. However, development of telomerase inhibitors has been challenging and thus far there are no clinically approved strategies exploiting this cancer target. The discovery of prevalent mutations in the TERT promoter region in many cancers and recent advances in telomerase biology has led to a renewed interest in targeting this enzyme. Here we discuss recent efforts targeting telomerase, including immunotherapies and direct telomerase inhibitors, as well as emerging approaches such as targeting TERT gene expression driven by TERT promoter mutations. We also address some of the challenges to telomerase-directed therapies including potential therapeutic resistance and considerations for future therapeutic applications and translation into the clinical setting. Although much work remains to be done, effective strategies targeting telomerase will have a transformative impact for cancer therapy and the prospect of clinically effective drugs is boosted by recent advances in structural models of human telomerase.

Indexed as

Molecular Targeted TherapyAnimalsBiomarkers, TumorClinical Studies as TopicDrug Evaluation, PreclinicalEnzyme InhibitorsGene Expression Regulation, NeoplasticHumansNeoplasmsTelomeraseTelomereTelomere HomeostasisTreatment OutcomeBiomarkers, TumorEnzyme InhibitorsTelomerase

Identifiers

PMID32733068
PMCPMC7678952
OpenAlexW3046047916

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.